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引用本文的文献

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本文引用的文献

1
It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4.是时候淘汰“血清学弱 D 表型”,并通过 RHD 基因分型来确定 D 血型,包括弱 D 4 型。
Transfusion. 2020 Apr;60(4):855-859. doi: 10.1111/trf.15741. Epub 2020 Mar 12.
2
Reliability of labeling red cell units with minor antigen historical results and process considerations.红细胞单位用次要抗原历史结果和过程考虑因素标记的可靠性。
Transfusion. 2020 Apr;60(4):822-830. doi: 10.1111/trf.15699. Epub 2020 Feb 22.
3
American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support.美国血液学会 2020 年镰状细胞病指南:输血支持。
Blood Adv. 2020 Jan 28;4(2):327-355. doi: 10.1182/bloodadvances.2019001143.
4
Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies.巴西镰状细胞病患者中不明原因 Rh 抗体的 RH 多样性和输血支持。
Transfusion. 2019 Oct;59(10):3228-3235. doi: 10.1111/trf.15479. Epub 2019 Aug 13.
5
Alloimmunization in patients with sickle cell disease and underrecognition of accompanying delayed hemolytic transfusion reactions.镰状细胞病患者的同种免疫反应和伴随的迟发性溶血性输血反应的漏诊。
Transfusion. 2019 Jul;59(7):2282-2291. doi: 10.1111/trf.15328. Epub 2019 Apr 25.
6
genotype matching for transfusion support in sickle cell disease.用于镰状细胞病输血支持的基因型匹配。
Blood. 2018 Sep 13;132(11):1198-1207. doi: 10.1182/blood-2018-05-851360. Epub 2018 Jul 19.
7
Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.镰状细胞病患者及非洲裔巴西献血者中具有临床相关性的RHD-CE基因型
Blood Transfus. 2016 Sep;14(5):449-54. doi: 10.2450/2016.0275-15. Epub 2016 Apr 28.
8
Variant RH alleles and Rh immunisation in patients with sickle cell disease.镰状细胞病患者的RH等位基因变异与Rh免疫
Blood Transfus. 2015 Jan;13(1):72-7. doi: 10.2450/2014.0324-13. Epub 2014 Jun 19.
9
Molecular matching for Rh and K reduces red blood cell alloimmunisation in patients with myelodysplastic syndrome.Rh和K的分子匹配可降低骨髓增生异常综合征患者的红细胞同种免疫。
Blood Transfus. 2015 Jan;13(1):53-8. doi: 10.2450/2014.0332-13. Epub 2014 Jun 12.
10
How do we identify RHD variants using a practical molecular approach?我们如何使用实用的分子方法来鉴定 RHD 变异体?
Transfusion. 2014 Apr;54(4):962-9. doi: 10.1111/trf.12557. Epub 2014 Feb 28.

因输入的红细胞 Rh 表位改变导致的 Rh 抗体:7 例巴西患者的病例系列。

Rh antibodies as a result of altered Rh epitopes on transfused red cells: a case series of seven Brazilian patients.

机构信息

Unicamp Blood Centre, Campinas, San Paolo, Brazil.

出版信息

Blood Transfus. 2021 Sep;19(5):413-419. doi: 10.2450/2020.0073-20. Epub 2020 Oct 9.

DOI:10.2450/2020.0073-20
PMID:33085591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8486610/
Abstract

BACKGROUND

Rh antibodies produced by patients receiving Rh-matched RBC units may be associated with inheritance of altered RH alleles or a result of altered Rh epitopes on donor red blood cells (RBC). On this background, our aim was to evaluate unexpected Rh antibodies in Brazilian patients receiving regular transfusions and determine the clinical significance of the alloantibody produced.

MATERIAL AND METHODS

We investigated seven patients (5 with sickle cell disease, 1 with myelodysplastic syndrome and 1 with β-thalassaemia) with unexplained Rh antibodies. All patients had complete serological and molecular analyses. A lookback at the donor units transfused to these patients was performed and donors suspected of having Rh variants were recruited for further analysis. Laboratory and clinical findings were used to evaluate the clinical significance of the alloantibodies produced.

RESULTS

The unexpected Rh antibodies found in the patients were not linked to the expression of partial Rh phenotypes according to serological and molecular analyses. Anti-D was found in two patients, anti-C was found in one patient, anti-c was found in one patient and anti-e was found in three patients carrying conventional D, C, c and e antigens respectively. Serological and molecular analyses of donors' samples revealed that six donors whose RBC were transfused to these patients carried partial Rh antigens. Only one anti-e in a patient with β-thalassaemia was autoreactive and could not be explained by RH diversity in his donors. Three of the seven Rh antibodies were associated with laboratory and clinical evidence of a delayed haemolytic transfusion reaction or decreased survival of transfused RBC at first detection.

DISCUSSION

Our study provides evidence that patients exposed to RBC units from donors with Rh variants may develop antibodies and some of these may be of clinical significance.

摘要

背景

接受 Rh 型相合红细胞(RBC)单位输注的患者产生的 Rh 抗体可能与改变的 RH 等位基因遗传有关,或者是由于供者 RBC 上 Rh 表位改变所致。在此背景下,我们的目的是评估在接受常规输血的巴西患者中意外出现的 Rh 抗体,并确定产生的同种异体抗体的临床意义。

材料和方法

我们研究了 7 名(5 名患有镰状细胞病,1 名患有骨髓增生异常综合征,1 名患有β-地中海贫血)原因不明 Rh 抗体的患者。所有患者均进行了完整的血清学和分子分析。对这些患者输注的供者单位进行了回溯,并招募了疑似存在 Rh 变异的供者进行进一步分析。利用实验室和临床发现评估产生的同种异体抗体的临床意义。

结果

根据血清学和分子分析,患者中发现的意外 Rh 抗体与部分 Rh 表型的表达无关。两名患者发现抗-D,一名患者发现抗-C,一名患者发现抗-c,三名分别携带常规 D、C、c 和 e 抗原的患者发现抗-e。对供者样本的血清学和分子分析显示,输注给这些患者的 RBC 的 6 名供者携带部分 Rh 抗原。只有一名β-地中海贫血患者的抗-e 为自身反应性,不能用其供者的 RH 多样性来解释。7 种 Rh 抗体中有 3 种与实验室和临床证据表明迟发性溶血性输血反应或首次检测到输注 RBC 存活率降低有关。

讨论

我们的研究提供了证据表明,暴露于 Rh 变异供者 RBC 单位的患者可能会产生抗体,其中一些可能具有临床意义。